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Jesper Graakjaer · SciRah

Researcher profile · Semantic Scholar

Jesper Graakjaer

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Jesper Graakjaer — researcher profile on SciRah

h-index: 20
Works: 37
Citations: 1,676

Most-cited papers

The Werner syndrome helicase and exonuclease cooperate to resolve telomeric D loops in a manner regulated by TRF1 and TRF2.
Patricia L. Opresko, M. Otterlei, Jesper Graakjaer, P. Bruheim +5 more
2004Molecules and Cells328 citations Open access
Semantic Scholar
No Association Between Telomere Length and Survival Among the Elderly and Oldest Old
Claus Bischoff, H. Petersen, Jesper Graakjaer, K. Andersen-Ranberg +4 more
2006Epidemiology240 citations Open access
Semantic Scholar
The relative lengths of individual telomeres are defined in the zygote and strictly maintained during life
Jesper Graakjaer, L. Pascoe, H. Der-Sarkissian, G. Thomas +3 more
2004Aging Cell130 citations Open access
Semantic Scholar
The pattern of chromosome-specific variations in telomere length in humans is determined by inherited, telomere-near factors and is maintained throughout life.
Jesper Graakjaer, Claus Bischoff, L. Korsholm, Søren Holstebroe +4 more
2003Mechanisms of Ageing and Development126 citations
Semantic Scholar
The heritability of telomere length among the elderly and oldest-old.
Claus Bischoff, Jesper Graakjaer, H. Petersen, J. Hjelmborg +4 more
2005Twin Research and Human Genetics86 citations Open access
Semantic Scholar
Telomere stability and telomerase in mesenchymal stem cells.
N. Serakıncı, Jesper Graakjaer, S. Kølvraa
2008Biochimie80 citations
Semantic Scholar
Allele-specific relative telomere lengths are inherited
Jesper Graakjaer, H. Der-Sarkissian, Annette Schmitz, J. Bayer +3 more
2006Human Genetics76 citations
Semantic Scholar
17q12 deletion and duplication syndrome in Denmark—A clinical cohort of 38 patients and review of the literature
M. Rasmussen, E. Vestergaard, Jesper Graakjaer, Y. Petkov +7 more
2016American Journal of Medical Genetics. Part A69 citations
Semantic Scholar
The duplication 17p13.3 phenotype: Analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes
C. Curry, J. Rosenfeld, E. Grant, K. Gripp +38 more
2013American Journal of Medical Genetics. Part A65 citations Open access
Semantic Scholar
Ectopically hTERT expressing adult human mesenchymal stem cells are less radiosensitive than their telomerase negative counterpart.
N. Serakıncı, Rikke Christensen, Jesper Graakjaer, Claire J. Cairney +4 more
2007Experimental Cell Research56 citations Open access
Semantic Scholar
Dosage changes of a segment at 17p13.1 lead to intellectual disability and microcephaly as a result of complex genetic interaction of multiple genes.
C. Carvalho, S. Vasanth, M. Shinawi, Chad Russell +14 more
2014American Journal of Human Genetics43 citations Open access
Semantic Scholar
The distribution pattern of critically short telomeres in human osteoarthritic knees
M. Harbo, L. Bendix, A. Bay-Jensen, Jesper Graakjaer +5 more
2012Arthritis Research & Therapy41 citations Open access
Semantic Scholar
Telomere Length Among the Elderly and Oldest-Old
Claus Bischoff, Jesper Graakjaer, H. Petersen, B. Jeune +3 more
2005Twin Research and Human Genetics38 citations Open access
Semantic Scholar
Heart defects and other features of the 22q11 distal deletion syndrome.
C. Fagerberg, Jesper Graakjaer, U. D. Heinl, L. B. Ousager +6 more
2013European Journal of Medical Genetics37 citations
Semantic Scholar
Duplication in the Microtubule-Actin Cross-linking Factor 1 gene causes a novel neuromuscular condition
L. Jørgensen, Mai-Britt Mosbech, N. Færgeman, Jesper Graakjaer +2 more
2014Scientific Reports35 citations Open access
Semantic Scholar
The Pattern of Chromosome‐Specific Variations in Telomere Length in Humans Shows Signs of Heritability and Is Maintained through Life
Jesper Graakjaer, J. Londoño-Vallejo, Kaare Christensen, Steen Kølvraa
2006Annals of the New York Academy of Sciences32 citations
Semantic Scholar
Age-dependence of relative telomere length profiles during spermatogenesis in man.
P. Jørgensen, J. Fedder, S. Koelvraa, Jesper Graakjaer
2013Maturitas27 citations
Semantic Scholar
Microarray-Based Analysis of Methylation Status of CpGs in Placental DNA and Maternal Blood DNA – Potential New Epigenetic Biomarkers for Cell Free Fetal DNA-Based Diagnosis
L. Hatt, M. M. Aagaard, Jesper Graakjaer, C. Bach +4 more
2015PLoS ONE23 citations Open access
Semantic Scholar
A case study of "disorganized development" and its possible relevance to genetic determinants of aging.
R. Walker, L. Pakula, M. Sutcliffe, P. Kruk +2 more
2009Mechanisms of Ageing and Development23 citations
Semantic Scholar
Defining the phenotype associated with microduplication reciprocal to Sotos syndrome microdeletion
F. Novara, F. Stanzial, E. Rossi, F. Benedicenti +9 more
2014American Journal of Medical Genetics. Part A20 citations Open access
Semantic Scholar
Capsulorhexis contraction after cataract surgery: Comparison of sharp anterior edge and modified anterior edge acrylic intraocular lenses
C. Corydon, Michael E Lindholt, E. B. Knudsen, Jesper Graakjaer +2 more
2007Journal of cataract and refractive surgery17 citations
Semantic Scholar
Mesenchymal stem cells with high telomerase expression do not actively restore their chromosome arm specific telomere length pattern after exposure to ionizing radiation
Jesper Graakjaer, Rikke Christensen, S. Kølvraa, N. Serakıncı
2007BMC Molecular Biology16 citations Open access
Semantic Scholar
The Heritability of Telomere Length Among the Elderly and Oldest-Old
Claus Bischoff, Jesper Graakjaer, H. Petersen, J. Hjelmborg +4 more
2005Twin Research and Human Genetics15 citations Open access
Semantic Scholar
Mosaicism for copy number variations in the placenta is even more difficult to interpret than mosaicism for whole chromosome aneuploidy
Ida C. Bay Lund, N. Becher, Jesper Graakjaer, D. Lildballe +5 more
2021Prenatal Diagnosis14 citations Open access
Semantic Scholar
Syddansk Universitet Microarray-based analysis of methylation of 1 st trimester trisomic placentas from down syndrome , edwards syndrome and patau syndrome
L. Hatt, M. M. Aagaard, C. Bach, Jesper Graakjaer +3 more
201613 citations
Semantic Scholar
14q32.11 microdeletion including CALM1, TTC7B, PSMC1, and RPS6KA5: A new potential cause of developmental and language delay in three unrelated patients
Celeste C. Eno, Jesper Graakjaer, D. Svaneby, M. Nizon +4 more
2021American Journal of Medical Genetics. Part A8 citations Open access
Semantic Scholar
A Novel Pseudo-Dicentric Variant of 16p11.2–q11.2 Contains Euchromatin from 16p11.2–p11.1 and Resembles Pathogenic Duplications of Proximal 16q
J. C. K. Barber, Charlotte Brasch-Andersen, V. Maloney, Shuwen Huang +4 more
2012Cytogenetic and Genome Research6 citations
Semantic Scholar
Phylloid hypermelanosis in a child with psychomotor delay, cicatricial alopecia, hearing loss and polythelia.
A. Bygum, Y. Petkov, Jesper Graakjaer, U. Jensen +1 more
2012Acta Dermato-Venereologica6 citations Open access
Semantic Scholar
A case of penta X syndrome caused by nondisjunction in maternal meiosis 1 and 2
S. Markholt, Jesper Graakjaer, Signe Thim, Bente Høst +1 more
2017Clinical Case Reports3 citations Open access
Semantic Scholar
Prostaglandin E2‐EP3 receptor subtype gene deletion in mother and son impairs platelet aggregation
T. Goharian, C. Fagerberg, B. Jensen, Jesper Graakjaer +2 more
2019British Journal of Haematology1 citations Open access
Semantic Scholar
A novel myopathic condition caused by mutation of the macf1 gene locus
L. Jørgensen, M. Jensen, N. Færgeman, Jesper Graakjaer +2 more
20120 citations
Semantic Scholar
Syddansk Universitet Phylloid hypermelanosis in a child with psychomotor delay, cicatricial alopecia, hearing loss and polythelia Bygum,
A. Bygum, Y. Petkov, Jesper Graakjaer, U. Jensen +1 more
20120 citations
Semantic Scholar
An in vivo assessment of the relation between critical shortening of telomeres and osteoarthritis in humans: Telomeres and the DNA Damage Response. EMBO
M. Harbo, L. Bendix, A-C.b Jensen, Jesper Graakjaer +5 more
20100 citations
Semantic Scholar
206 CHONDROCYTE TELOMERE LENGTH DECREASES AS THE LEVEL OF CARTILAGE DEGENERATION IN HUMAN OSTEOATHRITIC KNEES INCREASES
M. Harbo, L. Bendix, A-C.b Jensen, Jesper Graakjaer +3 more
20080 citations Open access
Semantic Scholar
Universal STELA: an imrpoved method to measure the shortest telomeres
L. Bendix, Jesper Graakjaer, S. Kølvrå
20070 citations
Semantic Scholar
Allele-specific relative telomere lengths are inherited
Jesper Graakjaer, H. Der-Sarkissian, Annette Schmitz, J. Bayer +3 more
2006Human Genetics0 citations Open access
Semantic Scholar
A new potential cause of developmental and language delay in three unrelated patients
Eno Celeste Orcid ID 0000-0002-3857-9519, Celeste C. Eno, Jesper Graakjaer, D. Svaneby +5 more
0 citations
Semantic Scholar

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